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FDA 510(k)

AirLife 婴儿加热线电路

K号: K151303 · 2016-01-21

申请人Care Fusion
决定日期2016-01-21
产品代码BZE
咨询委员会AN 请注意,由于您没有提供完整的医疗设备监管文本,我无法提供完整的翻译。如果您能提供完整的文本,我将很乐意为您翻译。
决定实质等同

器械摘要

AirLife Infant Heated Wire Circuit is the device name listed in this FDA 510(k) record. The listed applicant is Care Fusion. It received FDA 510(k) clearance on 2016-01-21 under 510(k) number K151303. The device is classified under product code BZE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AirLife Infant Heated Wire Circuit?

AirLife Infant Heated Wire Circuit is a medical device that received FDA 510(k) clearance on 2016-01-21. The listed applicant is Care Fusion. The 510(k) number is K151303.

When did AirLife Infant Heated Wire Circuit receive FDA 510(k) clearance?

AirLife Infant Heated Wire Circuit received FDA 510(k) clearance on 2016-01-21, under 510(k) number K151303.

Who is the listed applicant for AirLife Infant Heated Wire Circuit?

The FDA 510(k) record lists Care Fusion as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AirLife Infant Heated Wire Circuit?

The FDA product code for AirLife Infant Heated Wire Circuit is BZE.

相关临床试验

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列明Care Fusion为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

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相关器械(代码:BZE)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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